ENST00000261937.11:c.3957G>T
MANE Select
|
ENSP00000261937.6:p.Arg1319=
|
|
ENST00000261937.10:c.3957G>T
|
ENSP00000261937.6:p.Arg1319=
|
|
ENST00000502603.5:n.657G>T
|
|
|
NM_182925.4:c.3957G>T
|
NP_891555.2:p.Arg1319=
|
|
XM_011534477.1:c.4206G>T
|
XP_011532779.1:p.Arg1402=
|
|
XM_011534478.1:c.4188G>T
|
XP_011532780.1:p.Arg1396=
|
|
XM_011534479.1:c.*103G>T
|
XP_011532781.1:n.*103G>T
|
|
XM_011534482.1:c.3975G>T
|
XP_011532784.1:p.Arg1325=
|
|
XM_011534483.1:c.3897G>T
|
XP_011532785.1:p.Arg1299=
|
|
XM_011534484.1:c.3498G>T
|
XP_011532786.1:p.Arg1166=
|
|
XR_941095.1:n.4243G>T
|
|
|
XM_011534478.3:c.4188G>T
|
XP_011532780.1:p.Arg1396=
|
|
XM_011534484.2:c.3498G>T
|
XP_011532786.1:p.Arg1166=
|
|
XM_017009263.1:c.*103G>T
|
XP_016864752.1:n.*103G>T
|
|
XM_017009268.1:c.3879G>T
|
XP_016864757.1:p.Arg1293=
|
|
XR_001742050.2:n.4447G>T
|
|
|
NM_182925.5:c.3957G>T
MANE Select
|
NP_891555.2:p.Arg1319=
|
|